Intervertebral Implant

ABSTRACT

An intervertebral implant having an upper and a lower closing plate designed to engage the vertebral end plates. The implant has a deformable body between the closing plates. Between the deformable body and closing plates are cover plates. A plurality of fiber windings run between the cover plates to hold together the cover plates and the deformable body.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.13/733,336 filed Jan. 3, 2013, which is a continuation of U.S. patentapplication Ser. No. 12/827,376 filed on Jun. 30, 2010, which is acontinuation of U.S. patent application Ser. No. 12/198,761, filed onAug. 26, 2008, now abandoned, which is a continuation of U.S. patentapplication Ser. No. 10/553,495, filed on Jul. 25, 2006, now U.S. Pat.No. 7,429,270, which is a National Stage application of PCT/CH03/00247,filed on Apr. 14, 2003, the entire disclosures of which are incorporatedherein by reference in their entireties.

TECHNICAL FIELD

The invention concerns an intervertebral implant.

BACKGROUND

An intervertebral disc prosthesis of the generic type is known from U.S.Pat. No. 4,911,718 Lee. This known intervertebral disc prosthesiscomprises a central core, that is so formed from a biocompatibleelastomer, such that it is roughly equivalent to the nucleus pulpous ofa natural intervertebral disc, as well as from a multi-layer laminatefrom fibres bound in an elastomer, arranged around the core. Eachlaminate layer has its own yarn system, so that a plurality of fibregroups are present. The fibres of the individual layers have variousorientations, whereby the angles of the fibres relative to the centralaxis of the intervertebral disc are in the range of ±20° and ±50°,preferably 0°, +45° and −45°.

From WO 90/00374 Klaue a hip prosthesis is known, the shaft of which ismade from a tubular mesh, i.e. a structure, that comprises at least twoseries of fibres crossing one another. In this application the interiorof the tubular mesh remains empty as the shaft of the femur component.

In the case of the prosthesis disclosed in U.S. Pat. No. 4,911,718 Lee,although the individual fibres are integrated in the laminate that ismade from an elastomer or another type of synthetic material, their endsare, however, adhered only to the end plates, so that they do notsurround the core and consequently, in the case of a radial expansion ofthe core, cannot accept any tensile force. When adhering the lateralwalls, cut out from the fibrous matrix compound, to the end plate, afixing of the integrated fibres on the end plate is quite difficult,only the cross-section of the fibre offers a contact surface for thechemical joint. Therefore increased stresses occur especially on thesejoining places of the fibres on the end plate.

Furthermore, in the case of Lee the length of the individual fibres isonly from the bottom cover plate to the top cover plate, whatcorresponds to the sheathing height or a diagonal of the projectedsheathing height. Thus the forces occurring can be reduced only alongthese lengths due to the transfer of the shearing force of the fibres tothe elastomer. Thus positions of increased stresses result at thefixings, i.e. on the ends of the fibres.

The prosthesis disclosed in WO 90/00374 Klaue comprises a system offibres, the individual fibres of which are not fixed on both ends, aswell as there is no deformable core. Therefore in the case of an axialcompression of the prosthesis the axial compression forces occurringcannot be transferred as tensile forces to the fibres.

From U.S. Pat. No. 3,867,728 Stubstad et al. an intervertebral discprosthesis is known, that has an elastomeric sandwich structure with afibre system. A disadvantage of this known prosthesis is that the fibresystem, joined with the cover plates, is either not embedded in thesheathing body or in another embodiment is embedded in a multi-layerlaminate of an elastomer.

SUMMARY

This is where the invention wants to provide remedy. The object of theinvention is to produce an intervertebral implant, that comprises afibre system joined with the cover plates, by virtue of which asheathing body, surrounding the central part and made from a homogeneousmaterial, will be reinforced.

The inventions achieves this objective with an intervertebral implant asdescribed herein.

The basic advantages, achieved by the invention, are that with theintervertebral implant according to the invention

the fibre system can be first wound around the central part andfollowing this poured into an elastomer forming the elastic sheathingbody, so that the sheathing, enveloping the central part, can be easilyproduced,

by applying the elastic material around the fibre system after itswinding, the anchoring of the fibre system is possible by various means,for example also on the opposing inner surfaces of the cover plates,

the central part allows a movement of both adjacent bodies of thevertebra in the case of a compression, flexion or extension, lateralbending and torsion,

the momentary centre of rotation or the momentary axes of rotation arenot determined by the intervertebral implant itself, and they canposition themselves according to the rule of minimum forces or momentsoccurring,

by varying the number of fibres in the circumferential direction, thecross-section of the fibres and the choice of material, the behaviour ofthe intervertebral implant can be so adjusted, that under varying loadsthe movements occur as in the case of the natural intervertebral disc,and

by varying the arrangement and the execution of the fibre system certainmovement limitations can be placed on the intervertebral implant, andfrom a certain deformation a limit region occurs, where despite thefurther increasing forces no deformation takes place or in the case ofmoments occurring the implant will no longer tilt.

The axial compression forces occurring under a load on the spinal columnare transmitted to the central part via the two end plates. Thecompression forces deform the central part situated between the two endplates, in particular an elastic formed body possibly present therein,in such a manner that the central part bulges radially. This expansionof the central part is restricted by the fibre system surrounding thecentral part and the radial compression forces arising can be absorbedby the fibre system as a tensile force. Thus a further, disadvantageousbulging of the central part can be limited. By anchoring the fibresystem in both cover plates, the intervertebral implant remains stableeven under the greatest loads and the fibre system is capable towithstand even considerable tensile forces.

In a preferred embodiment the entire fibre system is embedded in theelastic sheathing body, so that the fibre system does not necessarilyneed to be made from a biocompatible material.

In a further embodiment the fibre system is only partially embedded inthe elastic sheathing body, while the fibre system has a radialthickness δ relative to the central axis and the elastic sheathing bodyhas a radial thickness d, and the δ/d×100% ratio is in a range of 80%and 350%. By virtue of this the advantages can be achieved, that thelarge relative movements in the peripheral region of the cover platesoccurring during a flexion/extension movement or a lateral movement ofthe adjacent bodies of the vertebra are not subjected to a greatresistance by the elastic sheathing body and due to this the danger of afissure formation in the sheathing body is slighter.

The embedding of the fibre system in the elastic sheathing body can becarried out various embodiments in such a manner, that

a) the fibre system can be moved relative to the elastic material of thesheathing body, or

b) the fibre system cannot be moved relative to the elastic material ofthe sheathing body.

In yet another embodiment the entire fibre system is anchored on thecover plates, so that greater tensile forces can be accepted by thefibre system, and consequently the intervertebral implant obtains agreat torsional rigidity.

In another embodiment the sheathing body, accommodating the fibresystem, is made from an elastic, biocompatible material, preferably anelastomer, produced in particular based on polyurethane (PUR). However,silicone rubber, polyethylene, polycarbonate urethane (PCU) orpolyethylene terephthalate (PET) may also be used.

In yet another embodiment the central part is filled at least partiallywith an incompressible medium, preferably a liquid.

In another embodiment the central part comprises an incompressibleliquid core and an elastic formed body provided around it, while theliquid can be accommodated, for example, in a cavity provided in theformed body. This brings with it the advantage, that by virtue of theliquid core a mechanical behaviour of the intervertebral implant issimilar to that of a physiological intervertebral disc. The axialdeformation of the elastic central part will result in the radialexpansion of the incompressible liquid and consequently in the radialexpansion of the wall of the central part containing the fibre system.The tensile forces, occurring due to the radial expansion or the bulgingof the wall of the central part, are basically absorbed by the fibres.

The anchoring of the fibres on the cover plates can be carried out, forexample, in the following manner:

a) Mechanically by guiding the fibres designed as continuous fibresthrough grooves and over the external surfaces of the cover plates fromone groove to another one. Thus the fibres surround the central parttogether with the cover plates. By guiding the fibres in the grooves thefibre system can be so anchored on the cover plates, that in the case oftensile forces acting on the fibres no slipping of the fibres on thelateral sides is possible because the fibres can absorb only tensileforces,

b) Mechanically by a wedge-shaped construction of the grooves, so thatthe fibres extending from cover plate to cover plate can be firmlyclamped in the grooves, and/or

c) By adhering the fibre system on the cover plates.

In yet another embodiment of the intervertebral implant according to theinvention each cover plate comprises on its periphery a lateral surfaceand grooves distributed on the circumference and radially penetratinginto the lateral surfaces. The fibres, part of this fibre system, areguided through these grooves.

In a further embodiment the central part and the fibre system are joinedwith the cover plates in a form-locking manner.

In yet a further embodiment the fibre system is guided over the externalsurfaces of both cover plates, so that it will surround the central partas well as the cover plates.

When using an endless fibre, that covers the entire implant, thestresses preferably are distributed on the entire circumference of thiswinding. The fibre system is preferably in the form of a woven material,fabric or is knitted.

In another embodiment channels are mortised in the external surfaces ofthe cover plates to accommodate the fibre system.

In yet another embodiment the central part is essentiallyhollow-cylindrical, hollow-prismatic or is a body of rotation, anellipsoid, a partial sphere or barrel-shaped with an axis of rotationthat is coaxial with the central axis. Such designs secure the advantagethat the position of the rotation axes of the adjacent vertebral bodiescorrespond to the greatest possible extent to those of the naturalintervertebral disc.

The fibre system can be made, for example, from UHMWPE (ultra highmolecular weight polyethylene) or from PET (polyethylene terephthalate).

In another embodiment of the intervertebral implant according to theinvention, a closing plate intended and designed for contact on the baseplate or cover plate of the adjacent vertebral bodies is affixed on eachcover plate, each of the said closing plate having an external surfaceat right angles to the central axis with a macroscopic structure. Thestructure may be, for example, in the form of teeth. The macroscopicstructure allows a primary stabilisation of the intervertebral implantimmediately after the operation. Thus a mechanical anchoring of theintervertebral implant at a time when the growing of the bone on theintervertebral implant has not yet taken place, can be achieved.

In yet a further embodiment the woven material is formed from first andsecond fibres, wherein the first fibres include an angle α with thecentral axis and the second fibres include an angle β with the centralaxis. The angles for α or β are preferably between 15° and 60°.

In another embodiment the first and second fibres are interwoven withone another.

In yet another embodiment the elastic formed body has at right angles tothe central axis a cross-sectional surface F_(F), while the central parthas at right angles to the central axis a cross-sectional surface F_(M)and the F_(F)/F_(M) ratio of these two cross-sectional surfaces isbetween 30% and 65%.

In a further embodiment the elastic formed body is surrounded by asemi-permeable membrane, while in the interior of the elastic formedbody preferably physiological table salt solution is present.

With regard to the central axis the fibre system may be single-layeredor multi-layered, preferably 2-6 layered. Furthermore, the fibre systemcan be wound on the elastic formed body. The winding on the elasticformed body can be in two different directions, preferably rotationallysymmetrically.

In yet another further embodiment a closing plate can be fastened oneach cover plate, the closing plate having at right angles to thecentral axis an external surface with a macroscopic structure,preferably in the form of teeth.

The diameter of the fibres is in a range of 0.005 mm and 0.025 mm. Ayarn (roving) is preferably produced from a plurality of fibres, whereby500-2000 fibres form a yarn with a cross-sectional surface of 0.5 mm² to2 mm².

In those embodiments, wherein the fibre system has fibre sectionscrossing one another, in the case of flexion movements (flexion,extension, lateral flexion) of the patients some fibre sections will beunilaterally clamped and in case of shearing the fibre sectionsextending tangentially to the shearing direction absorb the forces.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention and developments of the invention are explained in detailin the following based on partially schematic illustrations of severalembodiments. They show in:

FIG. 1—a side view of an embodiment of the intervertebral implantaccording to the invention,

FIG. 2—a top view on the embodiment of the intervertebral implantaccording to the invention, illustrated in FIG. 1,

FIG. 3—a side view of another embodiment of the intervertebral implantaccording to the invention,

FIG. 4—a section through the embodiment of the intervertebral implantaccording to the invention, illustrated in FIG. 3,

FIG. 5 a—a perspective illustration of the fibre system of an embodimentof the intervertebral implant according to the invention,

FIG. 5 b—a top view on the fibre system illustrated in FIG. 5 a,

FIG. 6 a—a perspective illustration of the fibre system of an embodimentof the intervertebral implant according to the invention,

FIG. 6 b—a top view on the fibre system illustrated in FIG. 6 a, and

FIG. 7—a section through a further embodiment of the intervertebralimplant according to the invention.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

FIGS. 1 and 2 illustrate an embodiment of the intervertebral implant 1according to the invention, that comprises a top cover plate 3 and abottom cover plate 4, each with an external surface 7, 8 extending atright angles to the central axis 2 and having a lateral surface 21, 22on the periphery. Between the cover plates 3, 4 there is a central part10 provided with a central cavity 11 and a sheathing 12, that surroundsthe fibre system 5. For the purpose of anchoring the fibres 6 of thefibre system 5 on the cover plates 3, 4, each of the peripheral lateralsurfaces 21, 22 has grooves 18, distributed on the circumference andradially protruding into the lateral surfaces 21, 22, so that the fibresystem 5 can be anchored in these grooves 18. In the central cavity 11there is an elastically deformable formed body 9 with an incompressiblecore, preferably a liquid core 13. Due to the incompressibility of theliquid core 13 during a compression of the cover plates 3, 4 parallel tothe longitudinal axis 2, for example, the elastic formed body 9 and thesheathing 12 with the fibre system 5 will bulge radially, i.e. at rightangles to the longitudinal axis 2, consequently the fibres 6 will beunder tension.

FIGS. 3 and 4 illustrate an embodiment of the intervertebral implant 1according to the invention, that comprises two cover plates 3, 4,provided at right angles to the central axis 2, and an elasticallydeformable central part 10 situated between them. The central part 10comprises a hollow-cylindrical sheathing 12 that is coaxial with thecentral axis 2 and a central cavity 11. In the central cavity 11 anelastic formed body 9 with an incompressible core is provided,preferably a liquid core 13. The formed body 9 is surrounded by asemi-permeable membrane, whereas the sheathing 12, that surrounds thefibre system 5 and an elastic sheathing body 25 passed through by thefibre system 5, is made from a synthetic material. The closing plates14, 15 are firmly joined with the cover plates 3, 4 and have axiallyprotruding surfaces 16, 17, which can be brought to rest on the endplates of two adjacent bodies of the vertebra. The fibre system 5 isanchored on the cover plates 3, 4 and is integrated in the sheathing 12and its purpose is to absorb the forces on the central part 10, saidforces acting on the intervertebral implant 1 via the bodies of thevertebra adjacent to the closing plates 14, 15, i.e. torsional forcesdue to the rotation of the bodies of the vertebra about the central axis2 relative to one another or bending moments due to lateral bendingand/or flexion/extension of the spinal column. For example, acompression force, acting on the intervertebral implant 1 parallel tothe central axis 2, is transferred by closing plates 14, 15 via bothcover plates 3,4 to the central part 10, while as the result the elasticformed body 9 will bulge at right angles to the central axis 2. Thisexpansion movement of the elastic formed body 9 is transferred to thesheathing 12 with the fibre system 5 and contained by this. Since thefibre system 5 is anchored on the cover plates 3, 4, the compressionforce, acting transversely to the central axis 2, generates tensileforces in the fibres of the fibre system 5. The fibre system 5 in thiscase is made from synthetic fibres, preferably from UHMWPE-fibres (ultrahigh molecular weight polyethylene) or from PET (polyethyleneterephthalate) and comprises a mesh from first and second fibres 6 a, 6b, that are interwoven with one another. By doing so, the first fibres 6a include an angle α and the second fibres 6 b an angle β with thecentral axis 2. In the embodiment of the intervertebral implant 1according to the invention illustrated here, the angles α and β areequal and are between 15° and 60°. The fibres 6 a, 6 b are anchored onthe cover plates 3, 4 by means of grooves 18 that are arranged on thecircumference of the cover plates 3, 4 parallel to the central axis 2,so that the fibres 6 a, 6 b are passed through the grooves 18 and can beguided to the next groove 18 over the surfaces 7, 8 in a channel 19. Thecover plates 3, 4 are made from synthetic material, whereas the closingplates 14, 15, arranged externally, are made from titanium or a titaniumalloy. The externally arranged closing plates 14, 15 are joined with thecover plates 3, 4 either by form-locking or frictional locking. Inparticular they can be adhered or welded to one another.

In FIGS. 5 a and 5 b a fibre system 5 is illustrated according to anembodiment of the intervertebral implant 1 according to the invention,wherein the fibres 6 extending over the end plates 3, 4 form chords onthe circular surfaces 7, 8 of the cover plates 3, 4.

In FIGS. 6 a and 6 b a fibre system 5 is illustrated according to anembodiment of the intervertebral implant 1 according to the invention,wherein the fibres 6 extending over the end plates 3, 4 cross at thepoint of intersection of the central axis 2 and the end plates 3, 4.

When compared with the arrangement of the fibres 6 (FIGS. 6 a, 6 b), theguiding of the fibres 6 as chords (FIGS. 5 a, 5 b) over the surfaces 7,8 of the end plates 3, 4 has the following advantages:

due to the better distribution of the crossing points of the fibres 6 noconcentration will occur, especially between the external surfaces 7, 8of the cover plates 3, 4 and the closing plates 14, 15 (FIGS. 3 and 4),and

with the aid of a winding technique the fibre system 5 can besymmetrically produced relative the central axis 2 while theintervertebral implant 1 can be clamped in at the points of intersectionbetween the central axis 2 and the cover plates 3, 4.

FIG. 7 illustrates an embodiment, that differs from the embodimentillustrated in FIGS. 3 and 4 only by that the periphery of the sheathing12 provided on the central part 10 comprises an elastic sheathing body25 only partially passed through by the fibre system 5, the thickness ofthe sheathing body d being smaller than the radial thickness δ of thefibre system.

What is claimed:
 1. An intervertebral implant sized to be implantedbetween a lower endplate of an upper vertebra and an upper endplate ofan adjacent lower vertebra, the implant comprising: (a) an upper closingplate having an external surface for contacting the lower endplate ofthe upper vertebra and an opposing inner surface; (b) a lower closingplate having an external surface for contacting the upper endplate ofthe lower vertebra and an opposing inner surface; (c) a top cover platejoined to the upper closing plate, the top cover plate including a top,outer surface and an opposing bottom, inner surface, wherein the outersurface of the top cover plate faces the inner surface of the upperclosing plate; (d) a bottom cover plate joined to the lower closingplate, the bottom cover plate including a bottom, outer surface and anopposing top, inner surface, wherein the outer surface of the bottomcover plate faces the inner surface of the lower closing plate; (e) adeformable body located between the top and bottom cover plates having afirst side wall located between the inner surfaces of the bottom and topcover plates, wherein the deformable body is a separate part from thetop cover plate and the bottom cover plate; and (f) a continuous,uninterrupted fiber wound along a fiber path that extends sequentially(1) from beneath the inner surface of the top cover plate and (2) over aportion of the outer surface of the top cover plate between the innersurface of the upper closing plate and the outer surface of the topcover plate and (3) back past the inner surface of the top cover plateand (4) traversing the first side wall and (5) past the inner surface ofthe bottom cover plate and (6) over a portion of the outer surface ofthe bottom cover plate between the inner surface of the lower closingplate and the outer surface of the bottom cover plate and (7) back pastthe inner surface of the bottom cover plate and (8) traversing the firstside wall and again (9) passing from beneath the inner surface of thetop cover plate and (10) over a portion of the outer surface of the topcover plate between the inner surface of the upper closing plate and theouter surface of the top cover plate and (11) back past the innersurface of the top cover plate; wherein the continuous, uninterruptedfiber is located entirely between the inner surfaces of the upper andlower closing plates.
 2. The intervertebral implant of claim 1 whereinthe first side wall of the deformable body has a perimeter and thecontinuous, uninterrupted fiber is wound repeatedly along the fiber pathsuch that the continuous, uninterrupted fiber extends around the entiredistance of the perimeter.
 3. The intervertebral implant of claim 1wherein the continuous, uninterrupted fiber is located directly adjacentto the outer surface of the bottom cover plate and also directlyadjacent to the outer surface of the top cover plate.
 4. Theintervertebral implant of claim 1 wherein the upper and lower closingplates are manufactured from titanium or titanium alloy.
 5. Theintervertebral implant of claim 1 wherein the continuous, uninterruptedfiber is wound in a manner that restricts expansion of the deformablebody.
 6. The intervertebral implant of claim 1 wherein the continuous,uninterrupted fiber is wound in a manner that holds together thedeformable body and the separate top and bottom cover plates.
 7. Theintervertebral implant of claim 1 wherein the deformable body iselastically deformable.
 8. The intervertebral implant of claim 1 whereinthe top cover plate is joined to the upper closing plate by frictionallocking or form-locking.
 9. The intervertebral implant of claim 1wherein the top cover plate is joined to the upper closing plate bywelding.
 10. The intervertebral implant of claim 1 wherein the top andbottom cover plates have an outer periphery and the continuous,uninterrupted fiber is wound over the outer surface of the top coverplate from the periphery of the outer surface of the top cover plate andwherein the continuous, uninterrupted fiber is wound over the outersurface of the bottom cover plate from the periphery of the outersurface of the bottom cover plate.
 11. The intervertebral implant ofclaim 10 wherein the top and bottom cover plates have grooves locatedalong the periphery and wherein the continuous, uninterrupted fiber iswound through the grooves of both the top and bottom cover plates. 12.An intervertebral implant sized to be implanted between a lower endplateof an upper vertebra and an upper endplate of an adjacent lowervertebra, the implant comprising: (a) an upper closing plate having anexternal surface for contacting the lower endplate of the upper vertebraand an opposing inner surface; (b) a lower closing plate having anexternal surface for contacting the upper endplate of the lower vertebraand an opposing inner surface; (c) a top cover plate joined to the upperclosing plate, the top cover plate including a top, outer surface and anopposing bottom, inner surface, wherein the outer surface of the topcover plate faces the inner surface of the upper closing plate; (d) abottom cover plate joined to the lower closing plate, the bottom coverplate including a bottom, outer surface and an opposing top, innersurface, wherein the outer surface of the bottom cover plate faces theinner surface of the lower closing plate; (e) a deformable body locatedbetween the top and bottom cover plates having (1) an upper surfacefacing the bottom, inner surface of the top cover plate, (2) a lowersurface facing the top, inner surface of the bottom cover plate, and (3)a first side wall located between the upper and lower surfaces of thedeformable body, wherein the deformable body is a separate part from thetop cover plate and the bottom cover plate; and (f) a continuous,uninterrupted fiber wound along a fiber path that extends sequentially(1) from beneath the inner surface of the top cover plate and (2) over aportion of the outer surface of the top cover plate between the innersurface of the upper closing plate and the outer surface of the topcover plate and (3) back past the inner surface of the top cover plateand (4) traversing the first side wall and (5) past the inner surface ofthe bottom cover plate and (6) over a portion of the outer surface ofthe bottom cover plate between the inner surface of the lower closingplate and the outer surface of the bottom cover plate and (7) back pastthe inner surface of the bottom cover plate and (8) traversing the firstside wall and again (9) passing from beneath the inner surface of thetop cover plate and (10) over a portion of the outer surface of the topcover plate between the inner surface of the upper closing plate and theouter surface of the top cover plate and (11) back past the innersurface of the top cover plate; wherein the continuous, uninterruptedfiber is located entirely between the inner surfaces of the upper andlower closing plates.
 13. The intervertebral implant of claim 12 whereinthe first side wall of the deformable body has a perimeter and thecontinuous, uninterrupted fiber is wound repeatedly along the fiber patharound the entire distance of the perimeter.
 14. The intervertebralimplant of claim 12 wherein the continuous, uninterrupted fiber islocated directly adjacent to the outer surface of the bottom cover plateand also directly adjacent to the outer surface of the top cover plate.15. The intervertebral implant of claim 12 wherein the upper and lowerclosing plates are manufactured from titanium or titanium alloy.
 16. Theintervertebral implant of claim 12 wherein the continuous, uninterruptedfiber is wound in a manner that restricts expansion of the deformablebody.
 17. The intervertebral implant of claim 12 wherein the continuous,uninterrupted fiber is wound in a manner that holds together thedeformable body and the separate top and bottom cover plates.
 18. Theintervertebral implant of claim 12 wherein the deformable body iselastically deformable.
 19. The intervertebral implant of claim 12wherein the top cover plate is joined to the upper closing plate byfrictional locking or form-locking.
 20. The intervertebral implant ofclaim 12 wherein the top cover plate is joined to the upper closingplate by welding.
 21. The intervertebral implant of claim 12 wherein thetop and bottom cover plates have an outer periphery and the continuous,uninterrupted fiber is wound over the outer surface of the top coverplate from the periphery of the outer surface of the top cover plate andwherein the continuous, uninterrupted fiber is wound over the outersurface of the bottom cover plate from the periphery of the outersurface of the bottom cover plate.
 22. The intervertebral implant ofclaim 21 wherein the top and bottom cover plates have grooves locatedalong the periphery and wherein the continuous, uninterrupted fiber iswound through the grooves of both the top and bottom cover plates.